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Catalog Number:
17807
CAS Number:
182287-49-6
tert-Butoxycarbonylamino- (tetrahydropyran-4-yl)acetic acid
Purity:
≥ 95% (NMR)
Synonym(s):
N-Boc-2-(tetrahydropyran-4-yl)glycine
Documents
$52.88 /100MG
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Product Information

tert-Butoxycarbonylamino-(tetrahydropyran-4-yl)acetic acid is a versatile compound with significant applications in the field of organic synthesis and pharmaceutical development. This compound, often referred to as Boc-amino acid, is particularly valued for its protective group functionality, which is essential in peptide synthesis. Its unique structure allows for the selective protection of amino groups, facilitating the formation of complex molecules while minimizing unwanted side reactions. Researchers and industry professionals utilize this compound in the synthesis of various bioactive peptides and pharmaceuticals, enhancing the efficiency of their synthetic pathways.

Moreover, tert-Butoxycarbonylamino-(tetrahydropyran-4-yl)acetic acid offers notable advantages over similar protective groups due to its stability under a wide range of reaction conditions. This stability ensures that the compound can be employed in diverse chemical environments, making it an ideal choice for laboratories focused on drug discovery and development. Its application extends to the synthesis of intermediates in the production of therapeutic agents, providing a reliable solution for researchers aiming to streamline their synthetic processes.

Synonyms
N-Boc-2-(tetrahydropyran-4-yl)glycine
CAS Number
182287-49-6
Purity
≥ 95% (NMR)
Molecular Formula
C12H21NO5
Molecular Weight
259.3
MDL Number
MFCD04114473
PubChem ID
22309198
Appearance
White solid
Conditions
Store at 0-8°C
General Information
Synonyms
N-Boc-2-(tetrahydropyran-4-yl)glycine
CAS Number
182287-49-6
Purity
≥ 95% (NMR)
Molecular Formula
C12H21NO5
Molecular Weight
259.3
MDL Number
MFCD04114473
PubChem ID
22309198
Appearance
White solid
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

tert-Butoxycarbonylamino-(tetrahydropyran-4-yl)acetic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing chemists to selectively modify amino acids without affecting the rest of the molecule, thereby enhancing the efficiency of drug development.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in creating compounds that can improve bioavailability and target specificity in therapeutic applications.
  • Organic Synthesis: It is employed in various organic reactions, providing a versatile building block for synthesizing complex organic molecules, which is crucial in materials science and chemical engineering.
  • Biochemical Research: Researchers use this compound to study enzyme interactions and metabolic pathways, contributing to a deeper understanding of biological processes and potential therapeutic targets.
  • Analytical Chemistry: It is utilized in the development of analytical methods for detecting and quantifying specific compounds in complex mixtures, which is essential in quality control and regulatory compliance in the pharmaceutical industry.

Citations